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https://hdl.handle.net/11499/37197
Title: | Peripheral blood mononuclear cell microRNAs in coronary artery disease | Authors: | Sanlialp, M. Dodurga, Yavuz Uludag, B. Alihanoglu, Y.I. Enli, Yaşar Seçme, Mücahit Bostanci, H.E. |
Keywords: | CAD lipoprotein A miRNA angiotensin receptor antagonist beta adrenergic receptor blocking agent biological marker dipeptidyl carboxypeptidase inhibitor hydroxymethylglutaryl coenzyme A reductase inhibitor microRNA microRNA 145 microRNA 155 microRNA 21 microRNA 221 nitrate adult aged Article biochemical analysis controlled study coronary angiography coronary artery bypass surgery coronary artery disease coronary artery obstruction down regulation enzyme linked immunosorbent assay female gene expression human hypertension major clinical study male people by smoking status percutaneous coronary intervention peripheral blood mononuclear cell priority journal real time polymerase chain reaction RNA isolation |
Publisher: | Wiley-Liss Inc. | Abstract: | The accuracy of risk prediction for coronary artery disease can be improved with the use of novel molecular or genetic biomarkers. In this study, we investigated the difference of five selected microRNAs (miR or miRNA) in patients with coronary artery disease (CAD) and controls, assessed by coronary angiography. The study population consisted of 85 subjects, aged between 18 and 75 years and underwent invasive coronary angiography. Subjects with more than 30% stenosis in at least one coronary artery, patients with a history of prior percutaneous coronary intervention or coronary by-pass surgery were allocated to the patient group; whereas the subjects without at least 30% stenosis consisted the control group. Groups were similar in age, presence of hypertension, and smoking status. However, the proportion of males and subjects taking angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, beta blockers, nitrates, and statins were higher in the patient group. miR-221 and miR-155 were downregulated (P =.02 and.001, respectively), while miR-21 levels were significantly increased (P =.003) in the patient group compared to controls. Changes in miR-145 and miR-126 did not reach statistical significance (P >.05). miRNA- 21, miR-155, and miR-221 were differentially expressed between the patients and controls. miRNAs are promising biomarkers for CAD diagnosis, however, this requires further research with larger groups. © 2019 Wiley Periodicals, Inc. | URI: | https://hdl.handle.net/11499/37197 https://doi.org/10.1002/jcb.29557 |
ISSN: | 0730-2312 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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